Reported Mar 20, 2013 · Terminated
Cynch Lordotic T-PLlF Implant. Intervertebral fusion device with bone graft, for use with supplemental fixation.
Spine Smith Partners LP
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Spine Smith Partners LP · 93 Red River St · Austin, TX · 78701-4216
Is this the product you have?
- Cynch Lordotic T-PLlF Implant. Intervertebral fusion device with bone graft, for use with supplemental fixation.
- Lot codes and dates
- Part Number0609-2809-06
- Lot39AQ
- Amount recalled
- 3 units
Where it was sold
Why it was recalled
Implants were incorrectly laser marked as 23mm instead of 28mm.
This product could cause temporary or reversible health problems — stop using it.
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